| Presented Abstracts from the Twenty‐Seventh Annual Education Conference of the National Society of Genetic Counselors (Los Angeles, California, October 2008) |
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| A Quiet Revolution: The Birth of the Genetic Counselor at Sarah Lawrence College, 1969 |
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| Are Patient Rights to Information and Self‐Determination in Diagnostic Genetic Testing Upheld? A Comparison Of Patients’ and Providers’ Perceptions |
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| Life Trajectories, Genetic Testing, and Risk Reduction Decisions in 18–39 Year Old Women at Risk for Hereditary Breast and Ovarian Cancer |
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| A Systematic Review of the Effects of Disclosing Carrier Results Generated Through Newborn Screening |
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| Just Genes: The Ethics of Genetic Technologies |
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| Cowden Syndrome: A Critical Review of the Clinical Literature |
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| Perceptions of Familial Risk in those Seeking a Genetic Risk Assessment for Alzheimer's Disease |
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| Tools for Assessing Readability and Quality of Health‐Related Web Sites |
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| Before the Call |
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| How Parents Search, Interpret, and Evaluate Genetic Information Obtained from the Internet |
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"ethnically diverse" and "ethnicity" |
| Disease Rarity, Carrier Status, and Gender: A Triple Disadvantage for Women with Fabry Disease |
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| Is There a Significant Trend in Prevalence of Consanguineous Marriage in Tehran? A Review of Three Generations |
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| Decisions About Testing and Termination of Pregnancy for Different Fetal Conditions: A Qualitative Study of European White and Pakistani Mothers of Affected Children |
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European white / European women |
| Testing Teens: A Commentary |
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| Views on Abortion: A Comparison of Female Genetic Counselors and Women from the General Population |
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| Reflections About My Story and the Accompanying Commentary |
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| Diplomates Certified in 2007 |
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| Adolescent Carrier Testing in Practice: The Impact of Legal Rulings and Problems with “Gillick Competence” |
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| Standardized Human Pedigree Nomenclature: Update and Assessment of the Recommendations of the National Society of Genetic Counselors |
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| Commentary on “My Story: A Genetic Counselor's Journey from Provider to Patient” |
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| A Genetic Counselor's Journey from Provider to Patient: A Mother's Story |
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| What Patients and Their Relatives Think About Testing for BMPR2 |
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| Assessment of the Content and Process of Genetic Counseling: A Critical Review of Empirical Studies |
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| A Pilot Study of a Family History Risk Assessment Tool for Cardiovascular Disease |
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| The Stigmatising Implications of Presenting Schizophrenia as a Genetic Disease |
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| Psycho‐social Counselling in Predictive Genetic Testing for Cancer: The Association Between Number of Supportive Sessions and Client Characteristics as Assessed by Psycho‐social Workers |
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| Adolescent Carrier Testing in Practice: The Impact of Legal Rulings and Problems with “Gillick Competence” |
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| Living with Long QT Syndrome: A Qualitative Study of Coping with Increased Risk of Sudden Cardiac Death |
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| New Clinical Genetics, Andrew Read and Dian Donnai (Eds.) |
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| The Psychic Costs of Empathic Engagement: Personal and Demographic Predictors of Genetic Counselor Compassion Fatigue |
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| The Impact of Social Roles on the Experience of Men in <i>BRCA1/2</i> Families: Implications for Counseling |
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| Acculturation and Familiarity With, Attitudes Towards and Beliefs about Genetic Testing for Cancer Risk Within Latinas in East Harlem, New York City |
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| “What is this Genetics, Anyway?” Understandings of Genetics, Illness Causality and Inheritance Among British Pakistani Users of Genetic Services |
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British Pakistani |
| “I Wouldn't Classify Myself as a Patient”: The Importance of a “Well‐being” Environment for Individuals Receiving Counseling about Familial Cancer Risk |
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| The Relationship Between Psychological Distress and Personality in Women from Families with Familial Breast/Ovarian or Hereditary Non‐polyposis Colorectal Cancer in the Absence of Demonstrated Mutatio |
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| Genetic Testing of Children at Risk for Adult Onset Conditions: When is Testing Indicated? |
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| Editorial |
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| Family History of Pancreatic Cancer in a High‐Risk Cancer Clinic: Implications for Risk Assessment |
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Ashkenazi Jewish |
| Lessons Learned: Risk Management Issues in Genetic Counseling |
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| Diversity in Genetic Counseling: Past, Present and Future |
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African Americans, Hispanics and American Indians |
| Genetic Counseling in Southern Iran: Consanguinity and Reason for Referral |
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| Presented Abstracts from the Twenty‐Sixth Annual Education Conference of the National Society of Genetic Counselors (Kansas City, Missouri, October 2007) |
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| Promotion of Cancer Family History Awareness: Jameslink Cancer Risk Assessment Tool at Community Health Fairs |
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| Health Behaviors and Psychological Distress in Women Initiating <i>BRCA1/2</i> Genetic Testing: Comparison with Control Population |
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| A Qualitative Description of Receiving a Diagnosis of Clefting in the Prenatal or Postnatal Period |
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| Testicular Cancer and Genetics Knowledge Among Familial Testicular Cancer Family Members |
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| Culture and Acculturation Influences on Palestinian Perceptions of Prenatal Genetic Counseling |
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| Theology, Disability and the New Genetics: Why Science Needs the Church |
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| Experiences of Teens Living in the Shadow of Huntington Disease |
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| Genetics in Health Practice and Education Special Issue |
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| Cognitive and Behavioural Effects of Genetic Testing for Thrombophilia |
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| Role of Parenting Relationship Quality in Communicating about Maternal <i>BRCA1/2</i> Genetic Test Results with Children |
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| Impact of a Genetic Diagnosis of a Mitochondrial Disorder 5–17 Years After the Death of an Affected Child |
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| The Importance of Program Evaluation: How Can it be Applied to Diverse Genetics Education Settings? |
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| Genetics Education for Health Professionals: Strategies and Outcomes from a National Initiative in the United Kingdom |
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| Consumer Motivations for Pursuing Genetic Testing and their Preferences for the Provision of Genetic Services for Hearing Loss |
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| Secrets to Creating Effective and Interesting Educational Experiences: Tips and Suggestions for Clinical Educators |
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| Psychological Factors Associated with Emotional Responses to Receiving Genetic Risk Information |
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| Interactive Genetic Counseling Role‐Play: A Novel Educational Strategy for Family Physicians |
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| Mentoring Nurses in Familial Cancer Risk Assessment and Counseling: Lessons Learned From a Formative Evaluation |
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| Psychosocial Conditions of Women Awaiting Genetic Counseling: A Population‐based Study |
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| “Are You at Risk for Hereditary Breast Cancer?”: Development of a Personal Risk Assessment Tool for Hereditary Breast and Ovarian Cancer |
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| Diagnosis of Fabry Disease via Analysis of Family History |
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